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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154875Generated: October 28, 2026

Chloroacetyl chloride → HCID 86735835, compound

https://huagongshe.com/reaction/1154875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86735836HCID 86735836—
SolventDimethylacetamideHCID 31374—
ProductHCID 86735835HCID 8673583579%

Reaction Steps

To a solution of 2.43 g of ethyl α-ethoxyimino-2-aminothiazol-4-ylacetate hydrobromide in 25 ml of anhydrous N,N-dimethylacetamide is added 1.43 g of chloroacetyl chloride under cooling and stirring. The solution is stirred for 30 minutes under ice-cooling and then for 30 minutes at room temperature. To the reaction mixture is added 150 ml of ethyl acetate and the mixture is repeatedly washed with saturated aq. NaCl solution. The ethyl acetate layer is dried over anhydrous magnesium sulfate, and subjected to the distillation of the solvent under reduced pressure. To the residue is added water to precipitate solid material. The solid is collected by filtration and dried. The procedure gives 1.90 g of ethyl α-ethoxyimino-2-(chloroacetamino)-thiazol-4-ylacetate. Yield 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298606
Source datasetuspto-grants-1981_11
ORD IDord-5450f02c866f43aeb5fc427279db6e37
Source noteuspto-grants-1981_11